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A new, substituted palladacycle for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water.

ABSTRACT: A newly engineered palladacycle that contains substituents on the biphenyl rings along with the ligand HandaPhos is especially well-matched to an aqueous micellar medium, enabling valued Suzuki-Miyaura couplings to be run not only in water under mild conditions, but at 300 ppm of Pd catalyst. This general methodology has been applied to several targets in the pharmaceutical area. Multiple recyclings of the aqueous reaction mixture involving both the same as well as different coupling partners is demonstrated. Low temperature microscopy (cryo-TEM) indicates the nature and size of the particles acting as nanoreactors. Importantly, given the low loadings of Pd invested per reaction, ICP-MS analyses of residual palladium in the products shows levels to be expected that are well within FDA allowable limits.

SUBMITTER: Takale BS

PROVIDER: S-EPMC6849884 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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A new, <i>substituted</i> palladacycle for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water.

Takale Balaram S BS Thakore Ruchita R RR Handa Sachin S Gallou Fabrice F Reilly John J Lipshutz Bruce H BH

Chemical science 20190806 38

A newly engineered palladacycle that contains substituents on the biphenyl rings along with the ligand HandaPhos is especially well-matched to an aqueous micellar medium, enabling valued Suzuki-Miyaura couplings to be run not only in water under mild conditions, but at 300 ppm of Pd catalyst. This general methodology has been applied to several targets in the pharmaceutical area. Multiple recyclings of the aqueous reaction mixture involving both the same as well as different coupling partners is ...[more]

PMID: 31803456

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